ClinVar Miner

Variants studied for Dilated cardiomyopathy 1KK

Coded as:
Minimum submission review status: Collection method:
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Gene type:
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If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
32 15 605 393 57 1077

Gene and significance breakdown #

Total genes and gene combinations: 2
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Gene or gene combination pathogenic likely pathogenic uncertain significance likely benign benign total
MYPN 31 15 599 382 55 1058
LOC132089829, MYPN 1 0 6 11 2 19

Submitter and significance breakdown #

Total submitters: 20
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Submitter pathogenic likely pathogenic uncertain significance likely benign benign total
Invitae 26 11 588 381 52 1058
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center 0 0 3 11 18 32
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen 0 0 3 17 1 21
Genome Diagnostics Laboratory, University Medical Center Utrecht 0 0 2 5 8 15
ClinVar Staff, National Center for Biotechnology Information (NCBI) 0 2 13 0 0 15
Genome-Nilou Lab 0 0 0 0 10 10
OMIM 5 0 0 0 0 5
Centre for Mendelian Genomics, University Medical Centre Ljubljana 0 0 4 0 0 4
Baylor Genetics 0 0 2 0 0 2
Division of Human Genetics, Children's Hospital of Philadelphia 0 0 2 0 0 2
New York Genome Center 0 0 2 0 0 2
MGZ Medical Genetics Center 0 1 0 0 0 1
Mendelics 0 0 0 0 1 1
Genomic Research Center, Shahid Beheshti University of Medical Sciences 0 0 1 0 0 1
Center of Genomic medicine, Geneva, University Hospital of Geneva 0 1 0 0 0 1
Soonchunhyang University Bucheon Hospital, Soonchunhyang University Medical Center 0 0 1 0 0 1
Phosphorus, Inc. 0 0 1 0 0 1
Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard 0 0 0 0 1 1
3billion 1 0 0 0 0 1
Medizinische Genetik Mainz, Limbach Genetics GmbH 0 0 1 0 0 1

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